182 results on '"Rhead, Brooke"'
Search Results
2. Molecular profiling of a real-world breast cancer cohort with genetically inferred ancestries reveals actionable tumor biology differences between European ancestry and African ancestry patient populations
3. Author Correction: A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus.
4. Pharmacogenomic insights in psychiatric care: uncovering novel actionability, allele-specific CYP2D6 copy number variation, and phenoconversion in 15,000 patients
5. Genetic Ancestry and Somatic Mutations in Lung Adenocarcinoma: Insights from Real-World Clinico-Genomic Data
6. Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects
7. A phenotypic and genomics approach in a multi-ethnic cohort to subtype systemic lupus erythematosus.
8. Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology.
9. miRNA contributions to pediatric‐onset multiple sclerosis inferred from GWAS
10. Admixture mapping reveals evidence of differential multiple sclerosis risk by genetic ancestry.
11. Genetic risk factors for pediatric-onset multiple sclerosis.
12. Hypomethylation of CYP2E1 and DUSP22 Promoters Associated With Disease Activity and Erosive Disease Among Rheumatoid Arthritis Patients
13. Evidence for a causal relationship between low vitamin D, high BMI, and pediatric-onset MS
14. Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes
15. Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility.
16. Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk
17. UCSC Data Integrator and Variant Annotation Integrator
18. Imputation of race and ethnicity categories using genetic ancestry from real-world genomic testing data
19. Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome
20. The UCSC Genome Browser database: 2014 update
21. Pharmacogenomic Insights in Psychiatric Care: Uncovering Novel Actionability, Allele-Specific CYP2D6 Copy Number Variation, and Phenoconversion in 15,000 Patients
22. Imputation of race and ethnicity categories using continental genetic ancestry from real- world genomic testing data
23. Association of Genetic Ancestry with Molecular Tumor Profiles in Colorectal Cancer
24. Abstract 1923: Ancestry-associated differences in somatic mutation rates from tumor profiling data of a pan-cancer cohort of 100,000 patients
25. Abstract 1945: Racial disparities in comprehensive cancer tumor profiling testing from real-world data of 100,000 cancer patient records
26. Pharmacogenomic insights in psychiatric care: uncovering novel actionability, allele-specific CYP2D6copy number variation, and phenoconversion in 15,000 patients
27. Abstract C115: Racial disparities in tumor profiling testing inferred from continental genetic ancestry determination of 100,000 cancer patients
28. Computational Methods and Epidemiologic Approaches for Revealing the Etiology of Autoimmune Diseases
29. 132 Racial differences in TMB measures between paired tumor/normal and tumor-only sequencing across endometrial, bladder, and non-small cell lung cancers
30. Abstract 766: Genomic and transcriptomic comparison between breast cancers from patients of African and European genetically determined ancestries demonstrates potential for ancestry specific biomarker-informed therapies
31. Paired tumor/normal sequencing to overcome racial differences in tumor mutational burden (TMB).
32. Genetic ancestry differences in tumor mutation in early and average-onset colorectal cancer.
33. Genetic ancestry correlates of the cancer somatic mutational landscape from tumor profiling data of 50,000 patients with cancer.
34. eP485: Ancestry inference from targeted NGS tests to enable precision medicine and improve racial/ethnic representation in clinical trials
35. Racial and Ethnic Differences in Genomic Profiling of Early Onset Colorectal Cancer
36. Calling differential DNA methylation at cell-type resolution: addressing misconceptions and best practices
37. The UCSC Genome Browser database: extensions and updates 2013
38. The UCSC Genome Browser database: extensions and updates 2011
39. ENCODE whole-genome data in the UCSC Genome Browser: update 2012
40. The UCSC Genome Browser database: update 2011
41. ENCODE whole-genome data in the UCSC genome browser (2011 update)
42. Impact of genetic susceptibility to multiple sclerosis on the T cell epigenome: proximal and distal effects
43. Global expression and CpG methylation analysis of primary endothelial cells before and after TNFa stimulation reveals gene modules enriched in inflammatory and infectious diseases and associated DMRs
44. ENCODE whole-genome data in the UCSC Genome Browser
45. The UCSC Genome Browser database: update 2010
46. Variation resources at UC Santa Cruz
47. The ENCODE Project at UC Santa Cruz
48. 149 Network-based analysis of clinical and molecular data in a multiethnic lupus cohort identifies molecular associations with serological manifestations
49. Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients
50. Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biology
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